Canonical Allele Identifier: CA343772596

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873149G>T (hg19) ; chr1:g.173904011G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904011G>T , CM000663.2:g.173904011G>T	GRCh38
NC_000001.10:g.173873149G>T , CM000663.1:g.173873149G>T	GRCh37
NC_000001.9:g.172139772G>T	NCBI36
NG_012462.1:g.18368C>A , LRG_577:g.18368C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1273C>A MANE Select	ENSP00000356671.3:p.Arg425Ser
ENST00000367698.3:c.1273C>A	ENSP00000356671.3:p.Arg425Ser
ENST00000617423.4:c.658C>A	ENSP00000478688.1:p.Arg220Ser
NM_000488.3:c.1273C>A , LRG_577t1:c.1273C>A	NP_000479.1:p.Arg425Ser
XM_005245198.2:c.1129C>A	XP_005245255.1:p.Arg377Ser
NM_001365052.1:c.1129C>A	NP_001351981.1:p.Arg377Ser
NM_000488.4:c.1273C>A MANE Select	NP_000479.1:p.Arg425Ser
NM_001365052.2:c.1129C>A	NP_001351981.1:p.Arg377Ser
NM_001386302.1:c.1396C>A	NP_001373231.1:p.Arg466Ser
NM_001386303.1:c.1354C>A	NP_001373232.1:p.Arg452Ser
NM_001386304.1:c.1252C>A	NP_001373233.1:p.Arg418Ser
NM_001386305.1:c.1216C>A	NP_001373234.1:p.Arg406Ser
NM_001386306.1:c.1057C>A	NP_001373235.1:p.Arg353Ser